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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966686Generated: October 27, 2026

Sodium Thiosulfate → HCID 53236719, compound

https://huagongshe.com/reaction/1966686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantPotassium hydroxy sulfiteHCID 23707502—
Reactant4-(2-amino-pyrimidin-5-yl)-N1-tert-butyl-benzene-1,2-diamineHCID 58541899—
Reactant2-(2,4-Dimethyl-thiazol-5-yl)-5-methoxy-benzaldehydeHCID 58542002—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 53236719HCID 5323671943%

Reaction Steps

To a solution of 4-(2-amino-pyrimidin-5-yl)-N1-tert-butyl-benzene-1,2-diamine (100 mg, 0.39 mmol) in DMF (5 mL) is added 2-(2,4-dimethyl-thiazol-5-yl)-5-methoxy-benzaldehyde (144 mg, 0.58 mmol) at room temperature. Oxone (239 mg, 0.39 mmol) in H2O (1 mL) is added and the solution is stirred for 4 hours. Saturated sodium thiosulfate solution (5 mL) is added and the mixture is extracted with EtOAc (3×10 mL) and H2O (10 mL). The combined organic layer is dried with MgSO4 and is filtered. The filtrate is concentrated and the residue is purified by silica gel flash column chromatography eluting with 10% MeOH in CH2Cl2 to afford the title compound (81 mg, 43%) as a pale brown foam. LCMS (ESMS): m/z 485.72 (M++1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420655B2
Source datasetuspto-grants-2013_04
ORD IDord-cd15a7c7d9474ab8961fb4ebf8bd6bbd
Source noteuspto-grants-2013_04